New methods of gene delivery using lasers

Leading laser scientists at the University of St Andrews have developed a new method of delivering genes to cells using laser light. The new technique, which is cheap and powerful, could have important implications for future studies in biomedicine and healthcare.

Optical technology has huge potential for novel developments in the bio-medical field and St Andrews has outstanding research groups in this area. The new method -which involves a miniature violet laser -is cheap, simple, powerful and versatile. Its adaptability means it could have potentially wide medical applications including gene therapy, the delivery of anti-cancer agents and advanced studies of neuro-degenerative diseases.

The development, published today, is the work of a team of researchers from across the University – with key figures from the School of Physics and Astronomy, the School of Biology and The Bute Medical School.

Key researchers Lynn Paterson and Ben Agate of the School of Physics and Astronomy said:

“We believe we have only touched the surface with this technology: the method is simple and inexpensive and could have important bio-medical implications and should find wide use. Since it also has the potential to assist in the cellular delivery of other bio-molecules, we are now looking at other cell types to see how widely applicable the method proves to be.”

The study is part of a new interdisciplinary initiative funded by SHEFC (Scottish Higher Education Funding Council) and the EPSRC (Engineering and Physical Sciences Research Council) which aims to use light to enhance our understanding of biology and to develop new biomedical devices. Although other research groups have touched on this area, the St Andrews group have greatly simplified the technique by using an extremely simple and versatile miniature violet laser which is compatible with standard microscopes. The method is very powerful, and in contrast to other methods the team can select individual cells to be treated at will under the microscope.

The new technique involves the violet laser being focused onto cell membranes for a fraction of a second – this causes the membrane to open up, allowing foreign genes to enter. The cell’s internal mechanism causes the membrane of the cell to heal itself thus appearing to suffer no long-lasting damage. After inserting the genes, the team grew the cells, which appeared to remain healthy and multiplied normally. The presence of the inserted gene in the multiplied cells was then confirmed by observing the red/green fluorescent proteins produced by the ‘new’ gene.

The study is published today by Optics Express: http://www.opticsexpress.org

Comments

The opinions expressed here are the views of the writer and do not necessarily reflect the views and opinions of News Medical.
Post a new comment
Post

While we only use edited and approved content for Azthena answers, it may on occasions provide incorrect responses. Please confirm any data provided with the related suppliers or authors. We do not provide medical advice, if you search for medical information you must always consult a medical professional before acting on any information provided.

Your questions, but not your email details will be shared with OpenAI and retained for 30 days in accordance with their privacy principles.

Please do not ask questions that use sensitive or confidential information.

Read the full Terms & Conditions.

You might also like...
CNIC team develops a comprehensive set of genetic tools and mouse lines